Canonical Allele Identifier: PA916048874
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 666569
ClinVar RCV Id: RCV000824993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Trp571Ser
CA369588174
NM_001374258.1:c.1712G>C